Cargando…

SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls

Disclosure: J. Desai: None. L. Letourneau-Freiberg: None. M. Msall: None. M. Scott: None. R.N. Naylor: None. L. Philipson: None. S.W. Greeley: None. Background: Neonatal diabetes mellitus (NDM), diabetes with onset before 6-12 months of age, is most commonly caused from mutations in the ATP-dependen...

Descripción completa

Detalles Bibliográficos
Autores principales: Desai, Jui, Letourneau-Freiberg, Lisa, Msall, Michael, Scott, Megan, Nicole Naylor, Rochelle, Philipson, Louis, Greeley, Siri Atma W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555337/
http://dx.doi.org/10.1210/jendso/bvad114.949
_version_ 1785116632810520576
author Desai, Jui
Letourneau-Freiberg, Lisa
Msall, Michael
Scott, Megan
Nicole Naylor, Rochelle
Philipson, Louis
Greeley, Siri Atma W
author_facet Desai, Jui
Letourneau-Freiberg, Lisa
Msall, Michael
Scott, Megan
Nicole Naylor, Rochelle
Philipson, Louis
Greeley, Siri Atma W
author_sort Desai, Jui
collection PubMed
description Disclosure: J. Desai: None. L. Letourneau-Freiberg: None. M. Msall: None. M. Scott: None. R.N. Naylor: None. L. Philipson: None. S.W. Greeley: None. Background: Neonatal diabetes mellitus (NDM), diabetes with onset before 6-12 months of age, is most commonly caused from mutations in the ATP-dependent Potassium (KATP) channel genes: KCNJ11 (KCNJ11-NDM) or ABCC8. Because of brain expression of mutant KATP channels, a spectrum of neurodevelopmental difficulties have been described, such as developmental delay, epilepsy, and neonatal diabetes (DEND) syndrome, learning disorders, and Attention-deficit/hyperactivity disorder (ADHD). In order to understand more about specific challenges, we compared self- and parent/caregiver-reported grit, anxiety, and social responsiveness among participants with KCNJ11 mutations and their sibling controls. Methods: We recruited 12 families (12 KCNJ11-NDM participants and 10 sibling controls) through the University of Chicago Monogenic Diabetes Registry (www.monogenicdiabetes.org). Affected participants and sibling controls, and in some cases their parent/caregiver, completed the SCARED/SCAARED (anxiety), SRS-2 (social responsiveness) and Grit Scale (grit) surveys. Nonparametric analyses were performed using the Mann-Whitney U-test for group comparisons. Results: Individuals with KCNJ11-NDM had significantly worse social responsiveness scores compared to sibling controls in both Total Social Responsiveness and 4/5 subscales including Social Awareness, Cognition, Communication, and Restricted Interests and Repetitive Behavior (p<0.05), but no difference for Motivation. In terms of deficits in social interaction, 20% of KCNJ11-NDM participants had total SRS-2 T-scores in the mild range, 30% with scores in the moderate range, and 40% with scores in the severe range. 80% of control participants had total SRS-2 T-scores in normal range. Grit results were not significantly different between groups. Total anxiety scores and anxiety subscale scores were not significantly different between groups. Nevertheless, both participants with KCNJ11-NDM and sibling controls revealed greater levels of anxiety as a whole; 50% of KCNJ11-NDM participants (n=6) and 40% of unaffected controls (n=4) had mean total anxiety scores ≥ 25, indicating the possible presence of a clinical anxiety disorder. Conclusion: The prevalence of social interaction challenges was high among KCNJ11-NDM participants, highlighting the importance of early clinical assessment and support for such problems. Results of the SRS-2 Motivation subscale and Grit, which measure more intrinsic levels of personality, may suggest that individuals with KCNJ11-NDM exhibit intrinsic motivation and grit. Elevated overall anxiety levels in both KCNJ11-NDM participants and sibling controls suggest the need for early assessment and supportive interventions for families affected by KCNJ11-NDM. Presentation: Saturday, June 17, 2023
format Online
Article
Text
id pubmed-10555337
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105553372023-10-06 SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls Desai, Jui Letourneau-Freiberg, Lisa Msall, Michael Scott, Megan Nicole Naylor, Rochelle Philipson, Louis Greeley, Siri Atma W J Endocr Soc Diabetes And Glucose Metabolism Disclosure: J. Desai: None. L. Letourneau-Freiberg: None. M. Msall: None. M. Scott: None. R.N. Naylor: None. L. Philipson: None. S.W. Greeley: None. Background: Neonatal diabetes mellitus (NDM), diabetes with onset before 6-12 months of age, is most commonly caused from mutations in the ATP-dependent Potassium (KATP) channel genes: KCNJ11 (KCNJ11-NDM) or ABCC8. Because of brain expression of mutant KATP channels, a spectrum of neurodevelopmental difficulties have been described, such as developmental delay, epilepsy, and neonatal diabetes (DEND) syndrome, learning disorders, and Attention-deficit/hyperactivity disorder (ADHD). In order to understand more about specific challenges, we compared self- and parent/caregiver-reported grit, anxiety, and social responsiveness among participants with KCNJ11 mutations and their sibling controls. Methods: We recruited 12 families (12 KCNJ11-NDM participants and 10 sibling controls) through the University of Chicago Monogenic Diabetes Registry (www.monogenicdiabetes.org). Affected participants and sibling controls, and in some cases their parent/caregiver, completed the SCARED/SCAARED (anxiety), SRS-2 (social responsiveness) and Grit Scale (grit) surveys. Nonparametric analyses were performed using the Mann-Whitney U-test for group comparisons. Results: Individuals with KCNJ11-NDM had significantly worse social responsiveness scores compared to sibling controls in both Total Social Responsiveness and 4/5 subscales including Social Awareness, Cognition, Communication, and Restricted Interests and Repetitive Behavior (p<0.05), but no difference for Motivation. In terms of deficits in social interaction, 20% of KCNJ11-NDM participants had total SRS-2 T-scores in the mild range, 30% with scores in the moderate range, and 40% with scores in the severe range. 80% of control participants had total SRS-2 T-scores in normal range. Grit results were not significantly different between groups. Total anxiety scores and anxiety subscale scores were not significantly different between groups. Nevertheless, both participants with KCNJ11-NDM and sibling controls revealed greater levels of anxiety as a whole; 50% of KCNJ11-NDM participants (n=6) and 40% of unaffected controls (n=4) had mean total anxiety scores ≥ 25, indicating the possible presence of a clinical anxiety disorder. Conclusion: The prevalence of social interaction challenges was high among KCNJ11-NDM participants, highlighting the importance of early clinical assessment and support for such problems. Results of the SRS-2 Motivation subscale and Grit, which measure more intrinsic levels of personality, may suggest that individuals with KCNJ11-NDM exhibit intrinsic motivation and grit. Elevated overall anxiety levels in both KCNJ11-NDM participants and sibling controls suggest the need for early assessment and supportive interventions for families affected by KCNJ11-NDM. Presentation: Saturday, June 17, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10555337/ http://dx.doi.org/10.1210/jendso/bvad114.949 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Diabetes And Glucose Metabolism
Desai, Jui
Letourneau-Freiberg, Lisa
Msall, Michael
Scott, Megan
Nicole Naylor, Rochelle
Philipson, Louis
Greeley, Siri Atma W
SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title_full SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title_fullStr SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title_full_unstemmed SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title_short SAT083 Comparing Grit, Anxiety, And Social Responsiveness In KCNJ11-NDM And Their Sibling Controls
title_sort sat083 comparing grit, anxiety, and social responsiveness in kcnj11-ndm and their sibling controls
topic Diabetes And Glucose Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555337/
http://dx.doi.org/10.1210/jendso/bvad114.949
work_keys_str_mv AT desaijui sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT letourneaufreiberglisa sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT msallmichael sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT scottmegan sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT nicolenaylorrochelle sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT philipsonlouis sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols
AT greeleysiriatmaw sat083comparinggritanxietyandsocialresponsivenessinkcnj11ndmandtheirsiblingcontrols